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US5290900A Expired / Lapsed US ⏱️ 0.0 years remaining

Curable fluorosilicone resin composition

Assignee: DuPont Toray Specialty Materials KK
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Filing: 1993-04-08
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Granted: 1994-03-01
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Expires: 2013-04-08
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Abstract

Abstract A curable fluorosilicone resin composition is disclosed, which composition comprises (A) 100 parts by weight of a fluorosilicone resin obtained by cohydrolyzing a mixture of (a) 50 to 95 mole percent of a perfluoroalkyl-containing organosilane having the formula R--CH 2 CH 2 SiX 3 , (b) 5 to 50 mole percent of an epoxy-containing organosilane having the formula Z w SiX 4-w and, optionally, (c) up to 50 mole percent of an organosilane having the formula R 1 n SiX 4-n , wherein R is a perfluoroalkyl group containing 4 to 15 carbon atoms, X is a hydrolyzable group, Z is an epoxy-containing monovalent organic group, R 1 is hydrogen or a monovalent hydrocabon group containing 1 to 15 carbon atoms, w is 1, 2 or 3 and n is 0, 1, 2 or 3; and (B) 1 to 50 parts by weight of a crosslinking agent selected from the group consisting of (i) an amino group-containing organosilicon compound that contains at least 2 nitrogen-bonded active hydrogens in each molecule and (ii) a fluorine compound that contains at least 2 carboxyl groups and at least 2 fluorine atoms in each molecule. When cured, the composition provides a film that is both highly water repellent and highly oil repellent.

Inventors

  • 👤 Hideki Kobayashi

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 08:56
CPC Classifications
C; C08; C08L; C08L83/00; C08L83/04; C08L83/08; C08G; C08G77/00; C08G77/04; C08G77/22; C08G77/24

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 187 words
A curable fluorosilicone resin composition comprising: (A) 100 parts by weight of a fluorosilicone resin obtained by cohydrolyzing a mixture of (a) 50 to 95 mole percent of a perfluoroalkyl-containing organosilane having the formula R--CH 2 CH 2 SiX 3 , (b) 5 to 50 mole percent of an epoxy-containing organosilane having the formula Z w SiX 4-w and, optionally, (c) up to 50 mole percent of an organosilane having the formula R 1 n SiX 4-n , wherein R is a perfluoroalkyl group containing 4 to 15 carbon atoms, X is a hydrolyzable group, Z is an epoxy-containing monovalent organic group, R 1 is hydrogen or a monovalent hydrocabon group containing 1 to 15 carbon atoms, w is 1, 2 or 3 and n is 0, 1, 2 or 3; and (B) 1 to 50 parts by weight of a crosslinking agent selected from the group consisting of (i) an amino group-containing organosilicon compound that contains at least 2 nitrogen-bonded active hydrogens in each molecule and (ii) a fluorine compound that contains at least 2 carboxyl groups and at least 2 fluorine atoms in each molecule.
Claim 2
Dependent Claim 187 words
A curable fluorosilicone resin composition comprising: (A) 100 parts by weight of a fluorosilicone resin obtained by cohydrolyzing a mixture of (a) 50 to 95 mole percent of a perfluoroalkyl-containing organosilane having the formula R--CH 2 CH 2 SiX 3 , (b) 5 to 50 mole percent of an epoxy-containing organosilane having the formula Z w SiX 4-w and, optionally, (c) up to 50 mole percent of an organosilane having the formula R 1 n SiX 4-n , wherein R is a perfluoroalkyl group containing 4 to 15 carbon atoms, X is a hydrolyzable group, Z is an epoxy-containing monovalent organic group, R 1 is hydrogen or a monovalent hydrocabon group containing 1 to 15 carbon atoms, w is 1, 2 or 3 and n is 0, 1, 2 or 3; and (B) 1 to 50 parts by weight of a crosslinking agent selected from the group consisting of (i) an amino group-containing organosilicon compound that contains at least 2 nitrogen-bonded active hydrogens in each molecule and (ii) a fluorine compound that contains at least 2 carboxyl groups and at least 2 fluorine atoms in each molecule.
Claim 3
Dependent Claim 44 words
The curable resin composition according to claim 1, wherein X of each said organosilane (a), (b) and (c) is a methoxy radical and said crosslinking agent (B) is an amino group-containing organosilicon compound that contains at least 2 nitrogen-bonded active hydrogens in each molecule.
Claim 4
Dependent Claim 28 words
The curable resin composition according to claim 2, wherein Z of said epoxy-containing organosilane (b) is selected from the group consisting of 3-glycidoxypropyl, 2-(3,4-epoxycyclohexyl)ethyl, 3-(3,4-epoxycyclohexyl)propyl, and 3,4-epoxycyclohexyl groups.
Claim 5
Dependent Claim 29 words
The curable resin composition according to claim 3, wherein said amino group-containing organosilicon compound is selected from the group consisting of 3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3-(2'-aminoethyl)aminopropyltrimethoxysilane, 3-(2'-aminoethyl)aminopropylmethyldimethoxysilane, 1,3-di(3'-aminopropyl)tetramethyldisiloxane, and 3-aminopropyldimethylsiloxy-endblocked polydimethylsiloxane.
Claim 6
Dependent Claim 17 words
The curable resin composition according to claim 4, wherein w of said epoxy-containing organosilane (b) is 1.
Claim 7
Dependent Claim 47 words
The curable resin composition according to claim 1, wherein X of each said organosilane (a), (b) and (c) is a methoxy radical and said crosslinking agent (B) is a fluorine compound that contains at least 2 carboxyl groups and at least 2 fluorine atoms in each molecule.
Claim 8
Dependent Claim 28 words
The curable resin composition according to claim 6, wherein Z of said epoxy-containing organosilane (b) is selected from the group consisting of 3-glycidoxypropyl, 2-(3,4-epoxycyclohexyl)ethyl, 3-(3,4-epoxycyclohexyl)propyl, and 3,4-epoxycyclohexyl groups.
Claim 9
Dependent Claim 30 words
The curable resin composition according to claim 3, wherein said fluorine compound is selected from the group consisting of tetrafluoroterephthalic acid, tetrafluorophthalic acid, tetrafluorosuccinic acid, octafluoroadipic acid and their anhydrides.
Claim 10
Dependent Claim 17 words
The curable resin composition according to claim 8, wherein w of said epoxy-containing organosilane (b) is 1.

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1997-02-28 1997-08-30 1998-03-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2001-02-28 2001-08-30 2002-03-01 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2005-02-28 2005-08-30 2006-03-01 $7700.00 Window Closed / Lapsed

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